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Journal Abstract Search

496 related items for PubMed ID: 11853367

  • 1. Mitochondrial 3243 BP mutation: a case report.
    Rigoli L, Caruso RA, Zuccarello D, Rigoli M, Barberi I.
    Diabetes Nutr Metab; 2001 Dec; 14(6):343-8. PubMed ID: 11853367
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  • 2. Functional and morphological abnormalities of mitochondria harbouring the tRNA(Leu)(UUR) mutation in mitochondrial DNA derived from patients with maternally inherited diabetes and deafness (MIDD) and progressive kidney disease.
    van den Ouweland JM, Maechler P, Wollheim CB, Attardi G, Maassen JA.
    Diabetologia; 1999 Apr; 42(4):485-92. PubMed ID: 10230654
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  • 4. [Analysis of mitochondrial DNA gene tRNALeu(UUR) A3243G mutation in diabetic pedigrees].
    Wang CL, Li F, Hou QZ, Li HZ, Zhang Y, Ning G.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Feb; 26(1):74-7. PubMed ID: 19199257
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  • 8. Maternally inherited diabetes and deafness: prevalence in a hospital diabetic population.
    Newkirk JE, Taylor RW, Howell N, Bindoff LA, Chinnery PF, Alberti KG, Turnbull DM, Walker M.
    Diabet Med; 1997 Jun; 14(6):457-60. PubMed ID: 9212310
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  • 10. Maternally inherited diabetes and deafness (MIDD): a distinct subtype of diabetes associated with a mitochondrial tRNA(Leu)(UUR) gene point mutation.
    van den Ouweland JM, Lemkes HH, Gerbitz KD, Maassen JA.
    Muscle Nerve Suppl; 1995 Jun; 3():S124-30. PubMed ID: 7603513
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  • 11. Maternally-inherited diabetes and deafness: report of two affected German families with the A3243G mitochondrial DNA mutation.
    Thorns C, Widjaja A, Boeck N, Skamira C, Zühlke H.
    Exp Clin Endocrinol Diabetes; 1998 Jun; 106(5):384-8. PubMed ID: 9831303
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  • 12. Molecular and clinical aspects of mitochondrial diabetes mellitus.
    Maassen JA, van Essen E, van den Ouweland JM, Lemkes HH.
    Exp Clin Endocrinol Diabetes; 2001 Jun; 109(3):127-34. PubMed ID: 11409293
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  • 13. A detailed investigation of maternally inherited diabetes and deafness (MIDD) including clinical characteristics, C-peptide secretion, HLA-DR and -DQ status and autoantibody pattern.
    Hosszúfalusi N, Karcagi V, Horváth R, Palik E, Várkonyi J, Rajczy K, Prohászka Z, Szentirmai C, Karádi I, Romics L, Pánczél P.
    Diabetes Metab Res Rev; 2009 Feb; 25(2):127-35. PubMed ID: 19116951
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  • 19. Maternally inherited diabetes and deafness is a distinct subtype of diabetes and associates with a single point mutation in the mitochondrial tRNA(Leu(UUR)) gene.
    van den Ouweland JM, Lemkes HH, Trembath RC, Ross R, Velho G, Cohen D, Froguel P, Maassen JA.
    Diabetes; 1994 Jun; 43(6):746-51. PubMed ID: 7910800
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